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Rifaximin Is Effective for the Treatment ofClostridium difficile—Associated Diarrhea: Results of an Open-Label Pilot Study

机译:利福昔明对治疗艰难梭菌相关性腹泻有效:一项开放性试验研究的结果

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Objectives. This open-label trial assessed the efficacy and safety of rifaximin as first-line therapy in hospitalized patients withClostridium difficile-associated diarrhea (CDAD).Methods. We enrolled thirteen patients who had a confirmed diagnosis of CDAD characterized by ≥3 unformed stools/day and positiveC. difficiletoxin assay. Those patients received rifaximin 400 mg three times daily for 10 days. Resolution of symptoms, repeat assay 10 days after treatment, and followup for recurrence were assessed.Results. Eight patients completed the study, and all reported symptom resolution during treatment. Mean time to last unformed stool was 132 h ± 42.5 h. Seven patients had no relapse by week 2 and in longer followup (median 162 days). One patient had recurrent CDAD during a repeat hospitalization.Conclusions. Rifaximin was effective and safe as first-line treatment for CDAD and did not result in recurrence in most patients.
机译:目标。这项开放性试验评估了利福昔明作为一线治疗在艰难梭菌相关性腹泻(CDAD)住院患者中的疗效和安全性。我们招募了13例确诊为CDAD的患者,这些患者特征在于每天≥3次未排便且阳性C。艰难梭菌毒素测定。这些患者每天接受3次400 mg利福昔明,共10天。评估症状缓解,治疗10天后重复测定以及随访复发情况。八名患者完成了研究,所有患者均报告了治疗期间的症状缓解。上一次未排便的平均时间为132 h±42.5 h。到第二周和更长的随访时间(中位162天),有7名患者没有复发。一名患者在再次住院期间复发了CDAD。利福昔明作为CDAD的一线治疗是有效和安全的,并且在大多数患者中不会导致复发。

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